JP7112839B2 - 発光素子、表示装置、電子機器、照明装置および有機化合物 - Google Patents
発光素子、表示装置、電子機器、照明装置および有機化合物 Download PDFInfo
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- JP7112839B2 JP7112839B2 JP2017219621A JP2017219621A JP7112839B2 JP 7112839 B2 JP7112839 B2 JP 7112839B2 JP 2017219621 A JP2017219621 A JP 2017219621A JP 2017219621 A JP2017219621 A JP 2017219621A JP 7112839 B2 JP7112839 B2 JP 7112839B2
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CN111836871A (zh) * | 2017-08-09 | 2020-10-27 | 学校法人冲绳科学技术大学院大学学园 | 长余辉组合物、长余辉元件及波长控制方法 |
WO2019069852A1 (ja) * | 2017-10-02 | 2019-04-11 | 国立大学法人九州大学 | 有機蓄光組成物および蓄光素子 |
CN110232298B (zh) * | 2018-03-05 | 2021-05-18 | 上海箩箕技术有限公司 | 光学指纹传感器模组 |
DE112019005603T5 (de) * | 2018-11-09 | 2021-07-22 | Semiconductor Energy Laboratory Co., Ltd. | Licht emittierende Vorrichtung, Licht emittierendes Gerät, Anzeigevorrichtung, elektronisches Gerät und Beleuchtungsvorrichtung |
KR102685451B1 (ko) * | 2018-12-03 | 2024-07-16 | 솔루스첨단소재 주식회사 | 유기 화합물 및 이를 포함하는 유기 전계 발광 소자 |
CN110061042B (zh) * | 2019-04-29 | 2021-02-02 | 上海天马微电子有限公司 | 一种显示面板和显示装置 |
US11659758B2 (en) | 2019-07-05 | 2023-05-23 | Semiconductor Energy Laboratory Co., Ltd. | Display unit, display module, and electronic device |
WO2021053787A1 (ja) * | 2019-09-19 | 2021-03-25 | シャープ株式会社 | 発光素子および表示デバイス |
TW202147665A (zh) * | 2020-04-28 | 2021-12-16 | 日商半導體能源研究所股份有限公司 | 發光器件、金屬錯合物、發光裝置、電子裝置及照明設備 |
US11690241B2 (en) | 2020-05-09 | 2023-06-27 | Shenzhen China Star Optoelectronics Semiconductor Display Technology Co., Ltd. | OLED with auxiliary electrode contacting electron transport layer |
CN111584564B (zh) * | 2020-05-09 | 2022-08-23 | 深圳市华星光电半导体显示技术有限公司 | 一种显示面板及显示面板制程方法 |
CN113045434B (zh) * | 2021-03-03 | 2022-11-29 | 陕西莱特光电材料股份有限公司 | 一种有机化合物以及使用其的有机电致发光器件和电子装置 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007251097A (ja) | 2006-03-20 | 2007-09-27 | Konica Minolta Holdings Inc | 有機エレクトロルミネッセンス素子、有機エレクトロルミネッセンス素子を用いた表示装置及び照明装置 |
WO2012001969A1 (ja) | 2010-06-30 | 2012-01-05 | 出光興産株式会社 | 芳香族アミン誘導体及びそれを用いた有機エレクトロルミネッセンス素子 |
JP2012216829A (ja) | 2011-03-30 | 2012-11-08 | Semiconductor Energy Lab Co Ltd | 発光素子 |
JP2012227524A5 (ko) | 2012-04-06 | 2015-04-30 |
Family Cites Families (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100490206C (zh) * | 2003-12-25 | 2009-05-20 | 华南理工大学 | 有机/高分子发光二极管 |
TW200541401A (en) | 2004-02-13 | 2005-12-16 | Idemitsu Kosan Co | Organic electroluminescent device |
WO2006001469A2 (en) * | 2004-06-23 | 2006-01-05 | Sharp Kabushiki Kaisha | Organic electroluminescence device, image display apparatus and lighting apparatus including the same charge transport material |
US8021763B2 (en) * | 2005-11-23 | 2011-09-20 | The Trustees Of Princeton University | Phosphorescent OLED with interlayer |
US7758972B2 (en) * | 2006-09-26 | 2010-07-20 | Semiconductor Energy Laboratory Co., Ltd. | Stilbene derivative, light emitting element, light emitting device, and electronic appliance |
WO2011027653A1 (en) * | 2009-09-04 | 2011-03-10 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting element, light-emitting device, and method for manufacturing the same |
DE202012013738U1 (de) * | 2011-02-16 | 2020-09-30 | Semiconductor Energy Laboratory Co., Ltd. | Lichtemittierendes Element |
TWI831058B (zh) | 2011-02-28 | 2024-02-01 | 日商半導體能源研究所股份有限公司 | 發光元件 |
KR20240100473A (ko) * | 2011-04-07 | 2024-07-01 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자 |
KR102026218B1 (ko) | 2011-11-25 | 2019-09-27 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자, 발광 장치, 전자 기기, 조명 장치, 및 유기 화합물 |
KR20140038886A (ko) * | 2012-09-21 | 2014-03-31 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자 |
KR101649683B1 (ko) | 2013-09-06 | 2016-08-19 | 제일모직 주식회사 | 유기광전자소자용 조성물, 유기 광전자 소자 및 표시 장치 |
KR101734459B1 (ko) | 2014-05-20 | 2017-05-11 | 제일모직 주식회사 | 유기 화합물, 조성물, 유기 광전자 소자 및 표시 장치 |
KR101792908B1 (ko) * | 2014-05-26 | 2017-11-02 | 주식회사 엘지화학 | 헤테로고리 화합물 및 이를 포함하는 유기 발광 소자 |
KR20230051628A (ko) * | 2014-09-30 | 2023-04-18 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자, 표시 장치, 전자 기기, 및 조명 장치 |
KR101818579B1 (ko) | 2014-12-09 | 2018-01-15 | 삼성에스디아이 주식회사 | 유기 광전자 소자 및 표시 장치 |
KR102295197B1 (ko) * | 2014-12-30 | 2021-09-01 | 엘티소재주식회사 | 화합물 및 이를 이용한 유기발광소자 |
TWI779405B (zh) * | 2015-03-09 | 2022-10-01 | 日商半導體能源研究所股份有限公司 | 發光元件,顯示裝置,電子裝置,與照明裝置 |
TWI837587B (zh) | 2015-05-21 | 2024-04-01 | 日商半導體能源研究所股份有限公司 | 發光元件、顯示裝置、電子裝置、及照明裝置 |
KR102697259B1 (ko) | 2015-05-21 | 2024-08-20 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자, 표시 장치, 전자 기기, 및 조명 장치 |
KR102655709B1 (ko) | 2015-07-21 | 2024-04-05 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자, 표시 장치, 전자 기기, 및 조명 장치 |
KR102236221B1 (ko) | 2015-07-23 | 2021-04-05 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자, 표시 장치, 전자 기기, 및 조명 장치 |
US10270039B2 (en) * | 2016-11-17 | 2019-04-23 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting element, display device, electronic device, and lighting device |
-
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Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007251097A (ja) | 2006-03-20 | 2007-09-27 | Konica Minolta Holdings Inc | 有機エレクトロルミネッセンス素子、有機エレクトロルミネッセンス素子を用いた表示装置及び照明装置 |
WO2012001969A1 (ja) | 2010-06-30 | 2012-01-05 | 出光興産株式会社 | 芳香族アミン誘導体及びそれを用いた有機エレクトロルミネッセンス素子 |
JP2012216829A (ja) | 2011-03-30 | 2012-11-08 | Semiconductor Energy Lab Co Ltd | 発光素子 |
JP2012227524A5 (ko) | 2012-04-06 | 2015-04-30 | ||
JP2014078699A5 (ko) | 2013-09-17 | 2016-09-23 |
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